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rs587781292

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781292(G;T)
Make rs587781292(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position61859868
GeneBRIP1
is asnp
is mentioned by
dbSNPrs587781292
ebirs587781292
HLIrs587781292
Exacrs587781292
Varsomers587781292
Maprs587781292
PheGenIrs587781292
hapmaprs587781292
1000 genomesrs587781292
hgdprs587781292
ensemblrs587781292
gopubmedrs587781292
geneviewrs587781292
scholarrs587781292
googlers587781292
pharmgkbrs587781292
gwascentralrs587781292
openSNPrs587781292
23andMers587781292
23andMe allrs587781292
SNP Nexus

SNPshotrs587781292
SNPdbers587781292
MSV3drs587781292
GWAS Ctlgrs587781292
Max Magnitude0
ClinVar
Risk rs587781292(A,T;A,T)
Alt rs587781292(A,T;A,T)
Reference rs587781292(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial cancer of breast not specified
Variation info
Gene BRIP1
CLNDBN Hereditary cancer-predisposing syndrome Familial cancer of breast not specified
Reversed 1
HGVS NC_000017.10:g.59937229C>A; NC_000017.10:g.59937229C>T
CLNSRC
CLNACC RCV000128992.2, RCV000196974.1, RCV000222594.1,